ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.1320C>G (p.Gly440=)

dbSNP: rs2144703498
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002138499 SCV002451084 likely benign MHC class II deficiency 2021-05-06 criteria provided, single submitter clinical testing

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